AU652874B2 - 5,6-disubstituted-3-pyridylmethyl ammonium halide compounds useful for the preparation of 5-(substituted methyl)-2, 3-pyridinedicarboxylic acids - Google Patents

5,6-disubstituted-3-pyridylmethyl ammonium halide compounds useful for the preparation of 5-(substituted methyl)-2, 3-pyridinedicarboxylic acids Download PDF

Info

Publication number: AU652874B2
Authority: AU; Australia
Prior art keywords: alkyl; groups; optionally substituted; halogen; hydrogen
Prior art date: 1991-12-20
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

AU30280/92A

Other languages

English (en)

Other versions

AU3028092A (en

Inventor

Henry Lee Strong

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Wyeth Holdings LLC

Original Assignee

American Cyanamid Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1991-12-20

Filing date

1992-12-18

Publication date

1994-09-08

1992-12-18 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1993-06-24 Publication of AU3028092A publication Critical patent/AU3028092A/en

1994-09-08 Application granted granted Critical

1994-09-08 Publication of AU652874B2 publication Critical patent/AU652874B2/en

2012-12-18 Anticipated expiration legal-status Critical

Status Expired legal-status Critical Current

Links

-1 5,6-disubstituted-3-pyridylmethyl ammonium halide compounds Chemical class 0.000 title claims abstract description 44
238000002360 preparation method Methods 0.000 title claims description 24
125000000217 alkyl group Chemical group 0.000 claims abstract description 47
229910052736 halogen Inorganic materials 0.000 claims abstract description 36
150000002367 halogens Chemical class 0.000 claims abstract description 36
125000003545 alkoxy group Chemical group 0.000 claims abstract description 20
229910052794 bromium Inorganic materials 0.000 claims abstract description 13
229910052801 chlorine Inorganic materials 0.000 claims abstract description 13
229910052740 iodine Inorganic materials 0.000 claims abstract description 6
101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 claims abstract 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 42
239000000203 mixture Substances 0.000 claims description 41
229910052739 hydrogen Inorganic materials 0.000 claims description 39
239000001257 hydrogen Substances 0.000 claims description 39
125000005843 halogen group Chemical group 0.000 claims description 35
238000000034 method Methods 0.000 claims description 35
150000001875 compounds Chemical class 0.000 claims description 32
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 29
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 24
150000002431 hydrogen Chemical class 0.000 claims description 22
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 20
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
239000002253 acid Substances 0.000 claims description 17
OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims description 17
239000002904 solvent Substances 0.000 claims description 16
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 15
239000000460 chlorine Substances 0.000 claims description 14
239000003795 chemical substances by application Substances 0.000 claims description 13
230000002140 halogenating effect Effects 0.000 claims description 13
229920006395 saturated elastomer Polymers 0.000 claims description 13
PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 claims description 12
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 12
125000004093 cyano group Chemical group *C#N 0.000 claims description 12
229910052757 nitrogen Inorganic materials 0.000 claims description 10
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 10
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 8
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
239000003999 initiator Substances 0.000 claims description 8
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 8
239000002585 base Substances 0.000 claims description 7
239000003960 organic solvent Substances 0.000 claims description 6
150000001412 amines Chemical group 0.000 claims description 5
125000000896 monocarboxylic acid group Chemical group 0.000 claims description 5
AISMNBXOJRHCIA-UHFFFAOYSA-N trimethylazanium;bromide Chemical compound Br.CN(C)C AISMNBXOJRHCIA-UHFFFAOYSA-N 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 3
150000004703 alkoxides Chemical class 0.000 claims description 3
230000003197 catalytic effect Effects 0.000 claims description 3
AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 claims description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
VRLDVERQJMEPIF-UHFFFAOYSA-N dbdmh Chemical compound CC1(C)N(Br)C(=O)N(Br)C1=O VRLDVERQJMEPIF-UHFFFAOYSA-N 0.000 claims description 2
QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 claims description 2
BBFCIBZLAVOLCF-UHFFFAOYSA-N pyridin-1-ium;bromide Chemical compound Br.C1=CC=NC=C1 BBFCIBZLAVOLCF-UHFFFAOYSA-N 0.000 claims description 2
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims description 2
NBNBICNWNFQDDD-UHFFFAOYSA-N sulfuryl dibromide Chemical compound BrS(Br)(=O)=O NBNBICNWNFQDDD-UHFFFAOYSA-N 0.000 claims 2
WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 claims 1
WERYHPXXOJWOCS-UHFFFAOYSA-N 5-(isoquinolin-2-ium-1-ylmethyl)pyridine-2,3-dicarboxylic acid;bromide Chemical compound [Br-].N1=C(C(O)=O)C(C(=O)O)=CC(CC=2C3=CC=CC=C3C=C[NH+]=2)=C1 WERYHPXXOJWOCS-UHFFFAOYSA-N 0.000 claims 1
101100285518 Drosophila melanogaster how gene Proteins 0.000 claims 1
101100135116 Oryza sativa subsp. japonica RR12 gene Proteins 0.000 claims 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
229910052751 metal Inorganic materials 0.000 claims 1
239000002184 metal Substances 0.000 claims 1
229910052760 oxygen Inorganic materials 0.000 abstract description 5
229910052717 sulfur Inorganic materials 0.000 abstract description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
239000007787 solid Substances 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
239000011541 reaction mixture Substances 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 8
239000000047 product Substances 0.000 description 8
238000010586 diagram Methods 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000004128 high performance liquid chromatography Methods 0.000 description 6
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 5
238000005481 NMR spectroscopy Methods 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 4
XTLNYNMNUCLWEZ-UHFFFAOYSA-N ethanol;propan-2-one Chemical compound CCO.CC(C)=O XTLNYNMNUCLWEZ-UHFFFAOYSA-N 0.000 description 4
238000010992 reflux Methods 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
238000000605 extraction Methods 0.000 description 3
239000012065 filter cake Substances 0.000 description 3
FKNQCJSGGFJEIZ-UHFFFAOYSA-N 4-methylpyridine Chemical compound CC1=CC=NC=C1 FKNQCJSGGFJEIZ-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
150000003973 alkyl amines Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
MKOJTLPEGLTEFM-UHFFFAOYSA-N dimethyl 5-methylpyridine-2,3-dicarboxylate Chemical compound COC(=O)C1=CC(C)=CN=C1C(=O)OC MKOJTLPEGLTEFM-UHFFFAOYSA-N 0.000 description 2
238000001914 filtration Methods 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000002002 slurry Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
229940086542 triethylamine Drugs 0.000 description 2
RQCOFILZZCGCOQ-UHFFFAOYSA-N (5,6-dicarboxypyridin-3-yl)methyl-trimethylazanium;bromide Chemical compound [Br-].C[N+](C)(C)CC1=CN=C(C(O)=O)C(C(O)=O)=C1 RQCOFILZZCGCOQ-UHFFFAOYSA-N 0.000 description 1
DDGHBOLOCQWPKE-UHFFFAOYSA-N 1,3-thiazole;hydrobromide Chemical compound [Br-].C1=CSC=[NH+]1 DDGHBOLOCQWPKE-UHFFFAOYSA-N 0.000 description 1
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
BPPSPXOWNGOEGL-UHFFFAOYSA-N 2-(4,5-dihydro-1h-imidazol-2-yl)pyridine Chemical class N1CCN=C1C1=CC=CC=N1 BPPSPXOWNGOEGL-UHFFFAOYSA-N 0.000 description 1
BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical class CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
UZHQHNDRVITJPL-UHFFFAOYSA-N 5,6-dimethoxy-1h-indole-2-carboxylic acid Chemical compound C1=C(OC)C(OC)=CC2=C1NC(C(O)=O)=C2 UZHQHNDRVITJPL-UHFFFAOYSA-N 0.000 description 1
XPQJONAGIGKDHD-UHFFFAOYSA-N 5-(2H-1,3-benzothiazol-2-ylium-1-ylmethyl)pyridine-2,3-dicarboxylic acid bromide Chemical compound [Br-].N1=C(C(O)=O)C(C(=O)O)=CC(CS=2[CH+]N=C3C=CC=CC3=2)=C1 XPQJONAGIGKDHD-UHFFFAOYSA-N 0.000 description 1
CJSGMWRJOBFTCK-UHFFFAOYSA-N 5-(methoxymethyl)pyridine-2,3-dicarboxylic acid Chemical compound COCC1=CN=C(C(O)=O)C(C(O)=O)=C1 CJSGMWRJOBFTCK-UHFFFAOYSA-N 0.000 description 1
KOSZAFIUTBOMSW-UHFFFAOYSA-N 5-(pyridin-1-ium-1-ylmethyl)pyridine-2,3-dicarboxylic acid;bromide Chemical compound [Br-].N1=C(C(O)=O)C(C(=O)O)=CC(C[N+]=2C=CC=CC=2)=C1 KOSZAFIUTBOMSW-UHFFFAOYSA-N 0.000 description 1
101150072179 ATP1 gene Proteins 0.000 description 1
101100003366 Arabidopsis thaliana ATPA gene Proteins 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
102100021649 Elongator complex protein 6 Human genes 0.000 description 1
241000490229 Eucephalus Species 0.000 description 1
101100065219 Homo sapiens ELP6 gene Proteins 0.000 description 1
101100338513 Mus musculus Hdac9 gene Proteins 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241001208007 Procas Species 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
101100338514 Xenopus laevis hdac9 gene Proteins 0.000 description 1
239000003957 anion exchange resin Substances 0.000 description 1
229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
101150105046 atpI gene Proteins 0.000 description 1
125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
239000007810 chemical reaction solvent Substances 0.000 description 1
ATQXMSAPMLWHBZ-UHFFFAOYSA-N chlorobenzene;propan-2-one Chemical compound CC(C)=O.ClC1=CC=CC=C1 ATQXMSAPMLWHBZ-UHFFFAOYSA-N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
KIDQHBXPNBCITQ-UHFFFAOYSA-N diethyl 5-methylpyridine-2,3-dicarboxylate Chemical group CCOC(=O)C1=CC(C)=CN=C1C(=O)OCC KIDQHBXPNBCITQ-UHFFFAOYSA-N 0.000 description 1
ZCDHDTQWOJRFFE-UHFFFAOYSA-N dimethyl 5-(methoxymethyl)pyridine-2,3-dicarboxylate Chemical compound COCC1=CN=C(C(=O)OC)C(C(=O)OC)=C1 ZCDHDTQWOJRFFE-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
OCLXJTCGWSSVOE-UHFFFAOYSA-N ethanol etoh Chemical compound CCO.CCO OCLXJTCGWSSVOE-UHFFFAOYSA-N 0.000 description 1
ZRSDQBKGDNPFLT-UHFFFAOYSA-N ethanol;oxolane Chemical compound CCO.C1CCOC1 ZRSDQBKGDNPFLT-UHFFFAOYSA-N 0.000 description 1
239000000284 extract Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
150000002466 imines Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
LVPMIMZXDYBCDF-UHFFFAOYSA-N isocinchomeronic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)N=C1 LVPMIMZXDYBCDF-UHFFFAOYSA-N 0.000 description 1
238000002955 isolation Methods 0.000 description 1
SHLPPXXKRFINFY-UHFFFAOYSA-N isoquinolin-2-ium;bromide Chemical compound Br.C1=NC=CC2=CC=CC=C21 SHLPPXXKRFINFY-UHFFFAOYSA-N 0.000 description 1
150000002537 isoquinolines Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
150000004885 piperazines Chemical class 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
150000003216 pyrazines Chemical class 0.000 description 1
HATXXVNYNPECAD-UHFFFAOYSA-N pyridazin-1-ium;bromide Chemical compound [Br-].C1=CC=[NH+]N=C1 HATXXVNYNPECAD-UHFFFAOYSA-N 0.000 description 1
PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
GJAWHXHKYYXBSV-UHFFFAOYSA-N pyridinedicarboxylic acid Natural products OC(=O)C1=CC=CN=C1C(O)=O GJAWHXHKYYXBSV-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
150000003235 pyrrolidines Chemical class 0.000 description 1
YHQSXWOXIHDVHQ-UHFFFAOYSA-N quinoline;hydrobromide Chemical compound [Br-].[NH+]1=CC=CC2=CC=CC=C21 YHQSXWOXIHDVHQ-UHFFFAOYSA-N 0.000 description 1
150000003248 quinolines Chemical class 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
238000010183 spectrum analysis Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003548 thiazolidines Chemical class 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pyridine Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Saccharide Compounds (AREA)

AU30280/92A 1991-12-20 1992-12-18 5,6-disubstituted-3-pyridylmethyl ammonium halide compounds useful for the preparation of 5-(substituted methyl)-2, 3-pyridinedicarboxylic acids Expired AU652874B2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US81252091A	1991-12-20	1991-12-20
US812520		2001-03-20

Publications (2)

Publication Number	Publication Date
AU3028092A AU3028092A (en)	1993-06-24
AU652874B2 true AU652874B2 (en)	1994-09-08

Family

ID=25209833

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AU30280/92A Expired AU652874B2 (en)	1991-12-20	1992-12-18	5,6-disubstituted-3-pyridylmethyl ammonium halide compounds useful for the preparation of 5-(substituted methyl)-2, 3-pyridinedicarboxylic acids

Country Status (20)

Country	Link
US (3)	US5288866A (fr)
EP (1)	EP0548532B1 (fr)
JP (1)	JP3107672B2 (fr)
KR (1)	KR100245586B1 (fr)
AT (1)	ATE151752T1 (fr)
AU (1)	AU652874B2 (fr)
BR (1)	BR9205097A (fr)
CA (1)	CA2085802C (fr)
CZ (2)	CZ286513B6 (fr)
DE (1)	DE69219089T2 (fr)
DK (1)	DK0548532T3 (fr)
ES (1)	ES2100261T3 (fr)
GR (1)	GR3023303T3 (fr)
HU (2)	HU218004B (fr)
IL (1)	IL104134A (fr)
MX (1)	MX9207270A (fr)
SG (1)	SG47555A1 (fr)
SK (2)	SK280466B6 (fr)
TW (1)	TW222267B (fr)
ZA (1)	ZA929877B (fr)

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SK283920B6 (sk)	1996-03-28	2004-05-04	Lonza Ag	Spôsob výroby arylamidov heteroaromatických karboxylových kyselín
US5900484A (en) *	1996-09-18	1999-05-04	Lonza Ag	Process for the preparation of arylamides of heteroaromatic carboxylic acids
ES2143816T3 (es) *	1996-05-09	2000-05-16	Lonza Ag	Procedimiento para la preparacion de arilamidas de acidos carboxilicos heteroaromaticos.
US5905154A (en) *	1996-06-10	1999-05-18	American Cyanamid Company	Process for the preparation of 5-(alkoxymethyl)-2,3-pyridinedicarboximide compounds
NZ314904A (en) *	1996-06-10	1998-06-26	American Cyanamid Co	Preparation of a herbicidal [(5,6-dicarboxy-3-pyridyl)methyl]ammonium halide
US5849916A (en) *	1996-06-10	1998-12-15	American Cyanamid Company	Process for the preparation of 2,3-pyridinedicarboximides
US6316629B1 (en)	1997-06-10	2001-11-13	American Cyanamid Co.	Process for the preparation of 2,3-pyridinedicarboximides
DK0820987T3 (da)	1996-07-23	2003-02-17	Lonza Ag	Fremgangsmåde til fremstilling af pyridin-2,3-dicarboxylsyreestere
CA2209392C (fr) *	1996-07-23	2007-02-20	Yves Bessard	Procede pour la preparation d'esters pyridinecarboxyliques
US6172117B1 (en)	1998-02-27	2001-01-09	Akzo Nobel N.V.	Biocidal preservatives
JP4685003B2 (ja) *	2003-07-02	2011-05-18	ビーエーエスエフソシエタス・ヨーロピア	酸化剤を用いたピリジン−２，３−ジカルボン酸エステルのｉｎ−ｓｉｔｕ処理
US7795439B2 (en) *	2004-06-25	2010-09-14	Basf Aktiengesellschaft	In-situ treatment of pyridine 2,3-dicarboxylic acid esters with an oxidizing agent
SG132562A1 (en)	2005-11-14	2007-06-28	Agency Science Tech & Res	Nano-positioning electromagnetic linear actuator
US7941953B2 (en) *	2006-01-17	2011-05-17	Bedford Industries, Inc.	Separable composite labeling articles in sheet or roll form
WO2010054952A1 (fr)	2008-11-13	2010-05-20	Basf Se	Acides 2-[(1-cyanopropyl)carbamoyl]-5-chlorométhylnicotiniques et leur utilisation dans la fabrication d'imidazolinones herbicides
BRPI0922087B1 (pt)	2008-11-13	2018-02-14	Basf Se	Processos para fabricar um composto e para preparar um composto
US9096570B2 (en) *	2008-11-13	2015-08-04	Basf Se	Process for manufacturing substituted 3-pyridylmethyl ammonium bromides
TWI506019B (zh) *	2008-12-08	2015-11-01	Basf Se	製造經取代５－甲氧基甲基吡啶－２，３－二羧酸衍生物之方法
EP2982673B1 (fr)	2008-12-09	2018-02-21	Basf Se	Procédé de fabrication d'anhydride de 5-chloromethyl-pyridine-2,3-dicarboxylique
ES2709063T3 (es) *	2016-08-15	2019-04-15	Helmholtz Zentrum Geesthacht	Composición inhibidora de la corrosión para magnesio o aleaciones de magnesio
UA125630C2 (uk)	2016-11-21	2022-05-04	Адама Аган Лтд.	Спосіб одержання метоксиметилпіридиндикарбоксилату
EP3782985A1 (fr)	2019-08-19	2021-02-24	BASF Agrochemical Products B.V.	Procédé de fabrication de dérivés d'acide 5-méthoxyméthylpyridine-2,3-dicarboxylique
CN117024406B (zh) *	2023-07-07	2026-03-06	江苏省农用激素工程技术研究中心有限公司	甲氧咪草烟的合成方法

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JPH0625116B2 (ja) *	1987-07-08	1994-04-06	ダイソー株式会社	ピリジン−２，３−ジカルボン酸誘導体の製造法
MY104933A (en) *	1987-09-30	1994-07-30	Pfizer Ltd	Platelet activating factor antagonists
DE3914969A1 (de) *	1989-05-02	1990-11-08	Schering Ag	5-substituierte 3-arylisoxazol-derivate, deren herstellung und verwendung als schaedlingsbekaempfungsmittel
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EP0461401A1 (fr) *	1990-06-15	1991-12-18	American Cyanamid Company	Procédé pour la préparation des esters dialcoyliques 2,3-dicarboxy-pyridine et leurs dérivés à partir des esters dichloromaléiques
US5125961A (en) *	1991-08-12	1992-06-30	Monsanto Company	Substituted pyridine compounds

1992
- 1992-10-14 US US07/960,749 patent/US5288866A/en not_active Expired - Lifetime
- 1992-11-16 EP EP92119537A patent/EP0548532B1/fr not_active Expired - Lifetime
- 1992-11-16 SG SG1996002817A patent/SG47555A1/en unknown
- 1992-11-16 DE DE69219089T patent/DE69219089T2/de not_active Expired - Lifetime
- 1992-11-16 DK DK92119537.6T patent/DK0548532T3/da active
- 1992-11-16 ES ES92119537T patent/ES2100261T3/es not_active Expired - Lifetime
- 1992-11-16 AT AT92119537T patent/ATE151752T1/de active
- 1992-11-26 TW TW081109493A patent/TW222267B/zh not_active IP Right Cessation
- 1992-12-15 MX MX9207270A patent/MX9207270A/es unknown
- 1992-12-15 SK SK3665-92A patent/SK280466B6/sk not_active IP Right Cessation
- 1992-12-15 CZ CS19923665A patent/CZ286513B6/cs not_active IP Right Cessation
- 1992-12-15 SK SK1400-98A patent/SK280477B6/sk not_active IP Right Cessation
- 1992-12-16 JP JP04353923A patent/JP3107672B2/ja not_active Expired - Lifetime
- 1992-12-17 IL IL104134A patent/IL104134A/xx not_active IP Right Cessation
- 1992-12-18 ZA ZA929877A patent/ZA929877B/xx unknown
- 1992-12-18 HU HU9602838A patent/HU218004B/hu unknown
- 1992-12-18 CA CA002085802A patent/CA2085802C/fr not_active Expired - Lifetime
- 1992-12-18 AU AU30280/92A patent/AU652874B2/en not_active Expired
- 1992-12-18 BR BR9205097A patent/BR9205097A/pt not_active IP Right Cessation
- 1992-12-18 HU HU9204021A patent/HU217563B/hu unknown
- 1992-12-19 KR KR1019920024795A patent/KR100245586B1/ko not_active Expired - Lifetime
1993
- 1993-11-22 US US08/156,205 patent/US5378843A/en not_active Expired - Lifetime
1994
- 1994-11-04 US US08/334,297 patent/US5545835A/en not_active Expired - Lifetime
1997
- 1997-04-09 CZ CZ19971082A patent/CZ286519B6/cs not_active IP Right Cessation
- 1997-05-02 GR GR960403251T patent/GR3023303T3/el unknown

Also Published As

Publication number	Publication date
SK140098A3 (en)	2000-02-14
HU9204021D0 (en)	1993-04-28
KR100245586B1 (ko)	2000-03-02
CZ286519B6 (cs)	2000-05-17
DE69219089T2 (de)	1997-07-24
HUT64052A (en)	1993-11-29
HU217563B (hu)	2000-02-28
IL104134A0 (en)	1993-05-13
CA2085802A1 (fr)	1993-06-21
JPH05255257A (ja)	1993-10-05
HU218004B (hu)	2000-05-28
SK280477B6 (sk)	2000-02-14
HK1001055A1 (en)	1998-05-22
DE69219089D1 (de)	1997-05-22
AU3028092A (en)	1993-06-24
EP0548532A1 (fr)	1993-06-30
CZ286513B6 (cs)	2000-05-17
ATE151752T1 (de)	1997-05-15
CZ366592A3 (en)	1993-08-11
GR3023303T3 (en)	1997-08-29
HU9602838D0 (en)	1996-11-28
SK366592A3 (en)	2000-02-14
SK280466B6 (sk)	2000-02-14
US5378843A (en)	1995-01-03
MX9207270A (es)	1993-07-01
DK0548532T3 (da)	1997-05-12
ZA929877B (en)	1993-07-02
JP3107672B2 (ja)	2000-11-13
US5545835A (en)	1996-08-13
KR930012748A (ko)	1993-07-21
EP0548532B1 (fr)	1997-04-16
ES2100261T3 (es)	1997-06-16
CA2085802C (fr)	2003-09-16
US5288866A (en)	1994-02-22
TW222267B (fr)	1994-04-11
IL104134A (en)	1997-06-10
BR9205097A (pt)	1993-06-22
SG47555A1 (en)	1998-04-17

Publication	Publication Date	Title
AU652874B2 (en)	1994-09-08	5,6-disubstituted-3-pyridylmethyl ammonium halide compounds useful for the preparation of 5-(substituted methyl)-2, 3-pyridinedicarboxylic acids
EP0509559B1 (fr)	2001-10-04	Amines alpha-insaturées, leur préparation et utilisation
US4069244A (en)	1978-01-17	Fluorinated amphoteric and cationic surfactants
NO168770B (no)	1991-12-23	Analogifremgangsmaate for fremstilling av terapeutisk aktive benzimidazolderivater
US4242516A (en)	1980-12-30	Fluorinated amphoteric surfactants
US5023336A (en)	1991-06-11	Imidazole compound and process for preparing the same
RU2090558C1 (ru)	1997-09-20	5,6-дизамещенные 3-пиридилметиламмоний галогениды, способ их получения и способы получения 5-(замещенный метил)-2,3-пиридиндикарбоновых кислот
CZ283485B6 (cs)	1998-04-15	Způsob výroby látek, antagonisujících receptory fibrinogenu
US5892050A (en)	1999-04-06	Process for the preparation of pyridine dicarboxylate derivatives
HU196377B (en)	1988-11-28	Process for production of 2-substituated-amin-5-acethilimidasoles
DK150511B (da)	1987-03-16	Fremgangsmaade til fremstilling af 3,4-di-hydro-4-oxo-2h-1,2-benzothiazin-3-carboxamid-1,1-dioxid-forbindelser
WO1983004252A1 (fr)	1983-12-08	Procede de preparation de pyridyl et quinolyl imidazolynones
US6087506A (en)	2000-07-11	Preparation of hetero arylcarboxamides
SU548204A3 (ru)	1977-02-25	Способ получени -(1-бис-арилкиламиноалкил)-аралкоксибензиловых спиртов или их солей, рацематов или оптическиактивных антиподов
HK1001055B (en)	1998-05-22	5,6-disubstituted-3-pyridylmethyl ammonium halide compounds useful for the preparation of 5-(substituted methyl)-2,3-pyridinedicarboxylic acids
US5106986A (en)	1992-04-21	Preparation of aminoethanol derivatives
KR100293858B1 (ko)	2001-09-17	2,5-이치환된피리딘의제조방법
IL93393A (en)	1994-10-07	Process for the preparation of omicron-carboxypyridyl and omicron-carboxyquinolyl- imidazolinones
US4923993A (en)	1990-05-08	Process for the preparation of 2-pyridinecarboxylic acid derivatives and 1-amino-1,4-dihydropyridine-2-carboxylic acid derivatives
US5541332A (en)	1996-07-30	Chloropyridinium chlorides and process for their preparation
JP3334309B2 (ja)	2002-10-15	６−アミノ−ニコチノニトリル類の製造方法
Kóródi	1991	Side‐chain chlorination of methylquinolines
US4526974A (en)	1985-07-02	Synthesis of 2-pyridylalkylamines
JPH01104041A (ja)	1989-04-21	Ｎ−［（２−オキソ−１−ピロリジニル）アセチル］ピペラジン誘導体、その製造方法および老人性痴呆症薬
AU7064491A (en)	1991-08-05	New thiazole derivatives